Prescott Jennifer, Karlson Elizabeth W, Orr Esther H, Zee Robert Y L, De Vivo Immaculata, Costenbader Karen H
From the Channing Division of Network Medicine, and the Division of Rheumatology, Allergy, and Immunology, and Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School; Program in Genetic Epidemiology and Statistical Genetics, Department of Epidemiology, Harvard TH Chan School of Public Health; Department of Pediatric Dentistry, Tufts University School of Dental Medicine, Boston, Massachusetts, USA.J. Prescott, PhD, Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and Program in Genetic Epidemiology and Statistical Genetics, Department of Epidemiology, Harvard TH Chan School of Public Health; E.H. Orr, BS, Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and Program in Genetic Epidemiology and Statistical Genetics, Department of Epidemiology, Harvard TH Chan School of Public Health; I. De Vivo, PhD, MPH, Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and Program in Genetic Epidemiology and Statistical Genetics, Department of Epidemiology, Harvard TH Chan School of Public Health; E.W. Karlson, MD, Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School; K.H. Costenbader, MD, MPH, Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School; R.Y. Zee, BDS, PhD, Division of Preventive Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, and Department of Pediatric Dentistry, Tufts University School of Dental Medicine.
J Rheumatol. 2016 Feb;43(2):282-8. doi: 10.3899/jrheum.150184. Epub 2016 Jan 15.
To prospectively examine the association between leukocyte telomere length (LTL) and subsequent rheumatoid arthritis (RA) development in women.
Using a case-control design nested within the prospective Nurses' Health Study (NHS), NHS II (NHSII), and Women's Health Study (WHS), each validated case of RA with a prediagnostic blood sample was matched to 3 controls by cohort, age, menopausal status, postmenopausal hormone therapy, and blood collection covariates. We measured telomere length in genomic DNA extracted from stored buffy coat samples using quantitative PCR. We used unconditional logistic regression to determine OR and 95% CI, and random-effects metaanalysis to combine study results.
In total, we analyzed 296 incident RA cases and 827 matched controls. Mean age of diagnosis among women who developed RA was 60.5 in NHS/NHSII and 61.3 in WHS. Metaanalysis demonstrated that longer prediagnostic LTL was associated with increased RA risk when women in the longest versus shortest LTL tertile were compared (OR 1.51, 95% CI 1.03-2.23, Pheterogeneity = 0.27). However, statistically significant between-study heterogeneity was observed for the intermediate tertile category (Pheterogeneity = 0.008). We did not observe heterogeneity by menopausal status, inflammatory cytokine levels, age at diagnosis, age at blood collection, body mass index, seropositivity, or HLA-DRβ1 shared epitope status.
Our results do not support an involvement for short LTL preceding RA development.
前瞻性研究女性白细胞端粒长度(LTL)与随后发生类风湿关节炎(RA)之间的关联。
采用巢式病例对照设计,纳入前瞻性护士健康研究(NHS)、NHS II(NHSII)和妇女健康研究(WHS)。将每例确诊前有血样的RA确诊病例按队列、年龄、绝经状态、绝经后激素治疗及采血协变量与3名对照进行匹配。我们使用定量PCR测量从储存的血沉棕黄层样本中提取的基因组DNA中的端粒长度。我们使用无条件逻辑回归确定比值比(OR)和95%置信区间(CI),并采用随机效应荟萃分析合并研究结果。
总共分析了296例新发RA病例和827名匹配对照。在NHS/NHSII中发生RA的女性的平均诊断年龄为60.5岁,在WHS中为61.3岁。荟萃分析表明,当比较最长与最短LTL三分位数的女性时,确诊前较长的LTL与RA风险增加相关(OR 1.51,95%CI 1.03 - 2.23,异质性P = 0.27)。然而,在中间三分位数类别中观察到研究间存在统计学显著异质性(异质性P = 0.008)。我们未观察到按绝经状态、炎症细胞因子水平、诊断年龄、采血年龄、体重指数、血清学阳性或HLA - DRβ1共享表位状态划分的异质性。
我们的结果不支持RA发生前短LTL的参与作用。